Hi all,
Regarding the clinic data of MSBB database (https://www.synapse.org/#!Synapse:syn6101474), for NP.1 column, how to decide whether the samples with 3 and 4 values AD or not in general.
Thanks
Hi,
I would like to know which are the scores of CDR and Braak that define a patient as AD or Control. This information is not entire clear to me.
Cheers,
Lukas Iohan @minghui.wang Thanks a lot! The classification was based on CDR, with controls (CDR = 0), MCI (CDR = 0.5) and AD (CDR > 0.5). Hi @minghui.wang
I have noticed that in your Scientific Data paper, table 2 shows there are 40 Controls, 43 MCIs, 258 ADs and 8 Unclassified. However there are no definitions of these groups in the paper.
I'd like to know the criteria of seperating samples into groups.
Thanks! Hi @minghui.wang @ben.logsdon,
I have another question about the MSBB covariates.
I have checked the ApoE information in the clinical file https://www.synapse.org/#!Synapse:syn6101474 (MSBB_clinical.csv), there are near 42% individuals missing ApoE information.
Do you have an update about the file?
Bests @ben.logsdon @minghui.wang Thanks for your answers. Ben's answer is correct. The MSBB AD cohort contains samples with a full spectrum of disease neuropathology and clinical outcomes. I wouldn't recommend treating the MSSB samples as simply AD or control.
Minghui Hi @boymin2020,
I believe that NP.1 indicates the CERAD score of the individual, which is a measure of amyloid pathology. @minghui.wang is that correct? Generally speaking NP.1, NFT, and clinical diagnosis (e.g. CDR) are combined to determine a diagnosis of AD.
Ben
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